Browsing by Subject "zebra finch"
Results Per Page
Sort Options
Item Embargo Dopamine Dynamics Drive Birdsong Learning(2024) Qi, JiaxuanWhile learning in response to extrinsic reinforcement is theorized to be driven by dopamine signals that encode the difference between expected and experienced rewards, skills that enable verbal or musical expression can be learned without extrinsic reinforcement. Instead, spontaneous execution of these skills is thought to be intrinsically reinforcing. Whether dopamine signals similarly guide learning of these intrinsically reinforced behaviors is unknown. Juvenile zebra finches are distinguished by their ability to copy the song of an adult tutor, a spontaneous, intrinsically reinforced process. Here, I use the zebra finch as a model system to study the neural mechanisms that operate within a song-specialized region of the basal ganglia (sBG) to enable this remarkable form of motor learning. Using in vivo microdialysis and computational methods to quantify juvenile song development, I first determined that dopamine (DA) signaling in the sBG is necessary for song learning. Using genetically encoded DA sensors and fiber photometry, I showed that DA dynamics in the sBG faithfully track the learned quality of juvenile song performance on a rendition-by-rendition basis. Consequently, my experiments provide compelling evidence that DA functions in the sBG as a reward prediction error-like signal to drive song learning, a process that evolves spontaneously and does not depend on extrinsic reward or punishment. Furthermore, I found that DA release in the sBG is driven not only by inputs from midbrain DA neurons classically associated with reinforcement learning but also by song premotor “cortical” inputs, which act via local cholinergic signaling in the sBG to elevate DA during singing. While I was able to show that both cholinergic and dopaminergic signaling in the sBG are necessary for song learning, I further found that only DA tracks the learned quality of song performance. Therefore, dopamine dynamics in the basal ganglia encode performance quality to drive self-directed and long-term learning of natural behaviors.
Item Open Access Mammalian genes induce partially reprogrammed pluripotent stem cells in non-mammalian vertebrate and invertebrate species.(Elife, 2013-09-03) Rosselló, Ricardo Antonio; Chen, Chun-Chun; Dai, Rui; Howard, Jason T; Hochgeschwender, Ute; Jarvis, Erich DCells are fundamental units of life, but little is known about evolution of cell states. Induced pluripotent stem cells (iPSCs) are once differentiated cells that have been re-programmed to an embryonic stem cell-like state, providing a powerful platform for biology and medicine. However, they have been limited to a few mammalian species. Here we found that a set of four mammalian transcription factor genes used to generate iPSCs in mouse and humans can induce a partially reprogrammed pluripotent stem cell (PRPSCs) state in vertebrate and invertebrate model organisms, in mammals, birds, fish, and fly, which span 550 million years from a common ancestor. These findings are one of the first to show cross-lineage stem cell-like induction, and to generate pluripotent-like cells for several of these species with in vivo chimeras. We suggest that the stem-cell state may be highly conserved across a wide phylogenetic range. DOI:http://dx.doi.org/10.7554/eLife.00036.001.Item Open Access Molecular profiling of the developing avian telencephalon: regional timing and brain subdivision continuities.(J Comp Neurol, 2013-11) Chen, Chun-Chun; Winkler, Candace M; Pfenning, Andreas R; Jarvis, Erich DIn our companion study (Jarvis et al. [2013] J Comp Neurol. doi: 10.1002/cne.23404) we used quantitative brain molecular profiling to discover that distinct subdivisions in the avian pallium above and below the ventricle and the associated mesopallium lamina have similar molecular profiles, leading to a hypothesis that they may form as continuous subdivisions around the lateral ventricle. To explore this hypothesis, here we profiled the expression of 16 genes at eight developmental stages. The genes included those that define brain subdivisions in the adult and some that are also involved in brain development. We found that phyletic hierarchical cluster and linear regression network analyses of gene expression profiles implicated single and mixed ancestry of these brain regions at early embryonic stages. Most gene expression-defined pallial subdivisions began as one ventral or dorsal domain that later formed specific folds around the lateral ventricle. Subsequently a clear ventricle boundary formed, partitioning them into dorsal and ventral pallial subdivisions surrounding the mesopallium lamina. These subdivisions each included two parts of the mesopallium, the nidopallium and hyperpallium, and the arcopallium and hippocampus, respectively. Each subdivision expression profile had a different temporal order of appearance, similar in timing to the order of analogous cell types of the mammalian cortex. Furthermore, like the mammalian pallium, expression in the ventral pallial subdivisions became distinct during prehatch development, whereas the dorsal portions did so during posthatch development. These findings support the continuum hypothesis of avian brain subdivision development around the ventricle and influence hypotheses on homologies of the avian pallium with other vertebrates.